Reported Dec 24, 2025 · Ongoing

Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number: 502-103 - Calf Implant style 1 size 3…

Dsaart LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: DSAART LLC · 2950 Arrowhead Dr · Carson City, NV · 89706-0488

Is this the product you have?

  • Brand NameAART
  • Calf Implant Product NameCalf
  • Implant Model/Catalog Number502-103 -
  • Calf Implant style 1 size 3 UDI-DI codeB490502103 502-104 -
  • Calf Implant style 1 size 4 UDI-DI codeB490502104 502-105 -
  • Calf Implant style 1 size 5 UDI-DI codeB490502105 502-106 -
  • Calf Implant style 1 size 6 UDI-DI codeB490502106 502-201 -
  • Calf Implant style 2 size 1 UDI-DI codeB490502201 502-303 -
  • Calf Implant style 3 size 3 UDI-DI codeB490502303 502-304 -
  • Calf Implant style 3 size 4 UDI-DI codeB490502304
Lot codes and dates

7 of 7 products

Products covered by this recall
Model / numberProduct as published
502-104Lot Numbers: 23-11-014 24-07-016 25-04-018 Model/ UDI-DI code: B490502104
502-105Lot Numbers: 24-02-011 24-07-017 25-04-003 Model/ UDI-DI code: B490502105
502-106Lot Number: 24-05-019 Model/ UDI-DI code: B490502106
502-201Lot Numbers: 24-09-006 24-12-011 Model/ UDI-DI code: B490502201
502-303Lot Number: 24-01-001 Model/ UDI-DI code: B490502303
502-304Lot Number: 23-06-019 Model/ UDI-DI code: B490502304
Lot Numbers: 24-12-013 25-03-005
Amount recalled
35 implants

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

Why it was recalled

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.